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Raimondo Maggi

Bio: Raimondo Maggi is an academic researcher from University of Parma. The author has contributed to research in topics: Catalysis & Heterogeneous catalysis. The author has an hindex of 39, co-authored 209 publications receiving 5647 citations. Previous affiliations of Raimondo Maggi include Imperial College London & Afyon Kocatepe University.


Papers
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Journal ArticleDOI
TL;DR: This Discussion concludes with a summary of the main findings of the 2016 Redox Deprotections Update, which confirmed the need for further investigation into the determinants of redoxdeprotection in relation to nitrogenous Derivatives.
Abstract: 2.7. Redox Deprotections 221 3. Thiol Protecting Groups 223 4. Carboxy Protecting Groups 223 4.1. Protection 224 4.2. Deprotection 226 5. Carbonyl Protecting Groups 227 5.1. Acetals 227 5.1.1. Protection 227 5.1.2. Deprotection 231 5.2. Dithioacetals 233 5.2.1. Protection 233 5.2.2. Deprotection 235 5.3. 1,3-Oxathiolanes 237 5.4. 1,1-Diacetates (Acylals) 238 5.4.1. Protection 238 5.4.2. Deprotection 239 5.5. Nitrogenous Derivatives 240 5.5.1. Protection 240 5.5.2. Deprotection 241 6. Amino Protecting Groups 242 6.1. Protection 242 6.2. Deprotection 244 7. Concluding Remarks 246 8. Acknowledgments 246 9. Abbreviations 246 10. References 246

388 citations

Journal ArticleDOI
TL;DR: In this paper, the reaction of aldehydes, β-dicarbonyl compounds and urea (Biginelli reaction) has been performed over solid acid catalysis, under solventless conditions or in water affording dihydropyrimidines in good yield and selectivity.

281 citations

Journal ArticleDOI
TL;DR: In this article, the synthesis of cyclic carbonates by CO2 insertion into epoxides catalysed by both homogeneous MTBD and TDB supported on MCM-41 mesoporous silica is reported.

211 citations


Cited by
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Journal ArticleDOI
TL;DR: Reaction Mechanism, Synthesis of Urea and Urethane Derivatives, and Alcohol Homologation 2382 10.1.
Abstract: 4.3. Reaction Mechanism 2373 4.4. Asymmetric Synthesis 2374 4.5. Outlook 2374 5. Alternating Polymerization of Oxiranes and CO2 2374 5.1. Reaction Outlines 2374 5.2. Catalyst 2376 5.3. Asymmetric Polymerization 2377 5.4. Immobilized Catalysts 2377 6. Synthesis of Urea and Urethane Derivatives 2378 7. Synthesis of Carboxylic Acid 2379 8. Synthesis of Esters and Lactones 2380 9. Synthesis of Isocyanates 2382 10. Hydrogenation and Hydroformylation, and Alcohol Homologation 2382

3,203 citations

Journal ArticleDOI
TL;DR: An overview of the preparation, properties, and potential applications of mesoporous organic-inorganic hybrid materials in the areas of catalysis, sorption, chromatography, and the construction of systems for controlled release of active compounds, as well as molecular switches, are given.
Abstract: Mesoporous organic-inorganic hybrid materials, a new class of materials characterized by large specific surface areas and pore sizes between 2 and 15 nm, have been obtained through the coupling of inorganic and organic components by template synthesis. The incorporation of functionalities can be achieved in three ways: by subsequent attachment of organic components onto a pure silica matrix (grafting), by simultaneous reaction of condensable inorganic silica species and silylated organic compounds (co-condensation, one-pot synthesis), and by the use of bissilylated organic precursors that lead to periodic mesoporous organosilicas (PMOs). This Review gives an overview of the preparation, properties, and potential applications of these materials in the areas of catalysis, sorption, chromatography, and the construction of systems for controlled release of active compounds, as well as molecular switches, with the main focus being on PMOs.

2,765 citations

Journal ArticleDOI
TL;DR: In this paper, a review of the preparation of ordered mesoporous catalysts is presented, and the essential properties of the resulting materials are described in the first part of this review.

1,994 citations

Journal ArticleDOI
Ulf Lindström1

1,477 citations

Journal ArticleDOI
TL;DR: The utilization of CO(2) as a building block may represent an interesting approach to synthetic methodologies less intensive in carbon and energy.
Abstract: The need to reduce the accumulation of CO2 into the atmosphere requires new technologies able to reduce the CO2 emission. The utilization of CO2 as a building block may represent an interesting approach to synthetic methodologies less intensive in carbon and energy. In this paper the general properties of carbon dioxide and its interaction with metal centres is first considered. The potential of carbon dioxide as a raw material in the synthesis of chemicals such as carboxylates, carbonates, carbamates is then discussed. The utilization of CO2 as source of carbon for the synthesis of fuels or other C1 molecules such as formic acid and methanol is also described and the conditions for its implementation are outlined. A comparison of chemical and biotechnological conversion routes of CO2 is made and the barriers to their exploitation are highlighted.

1,242 citations